MitMAB

Product Information

Molecular Formula:
C17H38BrN
Molecular Weight:
336.39
Description
MitMAB, an organic building block and cationic surfactant, is a dynamin inhibitor that inhibits the GTPase activity of dynamin I (Ki = 940 nM; IC50 = 3.1 μM). It has been used in a study to assess a surfactant-controlled synthetic method to obtain a nanophase of mesoporous ceria-zirconia solid solution containing cationic defects in the crystalline structure.
Synonyms
Tetradecyltrimethylammonium bromide; (1-Tetradecyl)trimethylammonium Bromide Cetrimide BP; MTAB ; Microcide II; Morpan T; Myristyltrimethylammonium bromide; Myrtrimonium Bromide; Mytab; N,N,N-Trimethyl-1-tetradecanaminium Bromide;N-Tetradecyl-N,N,N-trimethylammonium Bromide; Pentonium 4Br40;Quaternium 13; Querton 14Br40; TTAB; TTAB (surfactant); Tetradecyltrimethylammonium Bromide; Tetradonium Bromide; Trimethylmyristylammonium Bromide; n-Tetradecyltrimethylammonium Bromide
IUPAC Name
trimethyl(tetradecyl)azanium;bromide
Canonical SMILES
CCCCCCCCCCCCCC[N+](C)(C)C.[Br-]
InChI
InChI=1S/C17H38N.BrH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18(2,3)4;/h5-17H2,1-4H3;1H/q+1;/p-1
InChI Key
CXRFDZFCGOPDTD-UHFFFAOYSA-M
Melting Point
247.5°C
Purity
>98.0%(T)
Density
1.00±0.1 g/cm3
Solubility
Freely soluble in Chloroform, Ethanol (95%), Water; Practically insoluble in Ether
Appearance
White to Almost white powder to crystal
Application
Quaternary ammonium compounds are used in disinfectants and sanitizers to treat swimming pools and industrial water reservoirs, as antiseptics for cleaning wounds, skin, and burns, in hair conditioners, as softeners for textiles and paper, and as pigment dispersers.
Storage
Store at -20°C under inert atmosphere
Stability
Stable. Hygroscopic. Incompatible with strong oxidizing agents.

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
13
Exact Mass
335.21876 g/mol
Monoisotopic Mass
335.21876 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
158
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114032551-A Preparation method of ternary composite quaternary ammonium salt corrosion inhibitor 2022-01-12
CN-114013042-A UV curing method and curing device 2021-12-21
CN-114133576-A Polyphosphate flame retardant containing benzene ring structure and synthesis method thereof 2021-12-17
CN-114149062-A Bactericide for sulfate reducing bacteria in polymer-containing produced liquid and preparation method and application thereof 2021-12-17
CN-114045062-A Ceramic deinking agent, ceramic part deinking method and electronic equipment 2021-12-10
CN-114180545-A Copper removal method and method for preparing iron phosphate from waste lithium iron phosphate battery core powder 2021-12-10
CN-114163862-A Multilevel structure carbon material, preparation method thereof and anticorrosive paint 2021-12-07
CN-114086223-A Preparation method of acid bath, copper deposit and plating homogenizing agent 2021-12-06
CN-114058450-A Stable granular detergent composition and preparation method thereof 2021-12-03
CN-114149868-A Tablet detergent composition with hardness and solubility and preparation method thereof 2021-12-03

Literatures

PMID Publication Date Title Journal
23792315 2013-08-01 Synthesis, self-aggregation and biological properties of alkylphosphocholine and alkylphosphohomocholine derivatives of cetyltrimethylammonium bromide, cetylpyridinium bromide, benzalkonium bromide (C16) and benzethonium chloride European journal of medicinal chemistry
23062962 2013-01-01 Selective nanodecoration of modified cyclodextrin crystals with gold nanorods Journal of colloid and interface science
23022612 2012-12-01 Optical detection of NADH based on biocatalytic growth of Au-Ag core-shell nanoparticles Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
23079128 2012-12-01 Control filamentous bulking caused by chlorine-resistant Type 021N bacteria through adding a biocide CTAB Water research
23109107 2012-12-01 How to control the recombinant prion protein adhesion for successful storage through modification of surface properties Biointerphases
22977883 2012-11-07 Gold nanorods as surface enhanced Raman spectroscopy substrates for sensitive and selective detection of ultra-low levels of dithiocarbamate pesticides The Analyst
23003680 2012-11-05 Interactions of microbicide nanoparticles with a simulated vaginal fluid Molecular pharmaceutics
22552877 2012-11-01 An improved CTAB-ammonium acetate method for total RNA isolation from cotton Phytochemical analysis : PCA
23065669 2012-11-01 Post separation adjustment of pH to enable the analysis of aminoglycoside antibiotics by microchip electrophoresis with amperometric detection Electrophoresis
23066757 2012-10-25 In situ study of dynamic conformational transitions of a water-soluble poly(3-hexylthiophene) derivative by surfactant complexation The journal of physical chemistry. B
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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